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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848683Generated: October 26, 2026

5-Aminovaleric acid → 5-[[2-(Chloromethyl)-4-methyl-1-oxopentyl]amino]pentanoic acid

https://huagongshe.com/reaction/848683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminovaleric acidHCID 138—
Reactant2-(Chloromethyl)-4-methylvaleryl chlorideHCID 12769067—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product5-[[2-(Chloromethyl)-4-methyl-1-oxopentyl]amino]pentanoic acidHCID 20563967—

Reaction Conditions

Temperature5 °C

Reaction Steps

5-Aminovaleric acid (3.2 g) is dissolved in 15 ml of water containing 1.09 g of sodium hydroxide. This is cooled to 5° C. and 2-[chloromethyl]-4-methylvaleryl chloride in 30 ml of THF is added dropwise. The pH is maintained at 8-9 by the dropwise addition of 1.09 g sodium hydroxide in 20 ml of water as needed. After stirring for about 16 hours the reaction mixture is diluted with 30 ml of water and concentrated in vacuo to remove THF. The aqueous layer is washed with ether, and acidified with 10% hydrochloric acid. Product is extracted with ethyl acetate. The ethyl acetate is dried with magnesium sulfate, filtered and concentrated in vacuo to yield 4.3 g of product. Product is purified by chromatographing on 200 g of silica using as the solvent system 500 parts ether: 10 parts methanol: 5 parts acetic acid, yielding 2.0 g of material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297275
Source datasetuspto-grants-1981_10
ORD IDord-c8eb4d7ee286411b9faec544df72564a
Source noteuspto-grants-1981_10